Identification of EMT-related high-risk stage II colorectal cancer and characterisation of metastasis-related genes

被引:25
|
作者
Wang, Kai [1 ]
Song, Kai [1 ]
Ma, Zhigang [2 ]
Yao, Yang [2 ]
Liu, Chao [2 ]
Yang, Jing [1 ]
Xiao, Huiting [1 ]
Zhang, Jiashuai [1 ]
Zhang, Yanqiao [2 ]
Zhao, Wenyuan [1 ]
机构
[1] Harbin Med Univ, Dept Syst Biol, Coll Bioinformat Sci & Technol, Harbin 150086, Peoples R China
[2] Harbin Med Univ Canc Hosp, Dept Gastrointestinal Med Oncol, 150 Haping Rd, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
COLON-CANCER; EXPRESSION; SIGNATURES; IMPACT; TISSUE;
D O I
10.1038/s41416-020-0902-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Our laboratory previously reported an individual-level prognostic signature for patients with stage II colorectal cancer (CRC). However, this signature was not applicable for RNA-sequencing datasets. In this study, we constructed a robust epithelial-to-mesenchymal transition (EMT)- related gene pair prognostic signature. Methods Based on EMT-related genes, metastasis-associated gene pairs were identified between metastatic and non-metastatic samples. Then, we selected prognosis-associated gene pairs, which were significantly correlated with disease-free survival of stage II CRC using multivariate Cox regression model, as the EMT-related prognosis signature. Results An EMT-related signature composed of fifty-one gene pairs (51-GPS) for prediction-relapse risk of patients with stage II CRC was developed, whose prognostic efficiency was validated in independent datasets. Moreover, 51-GPS achieved better predictive performance than other reported signatures, including a commercial signature Oncotype Dx colon cancer and an immune-related gene pair signature. Besides, EMT-related functional gene sets achieved high enrichment scores in high-risk samples. Especially, loss-of-function antisense approach showed that DEGs between the predicted two clusters were metastasis-related. Conclusions The EMT-related gene pair signature can identify the high relapse-risk patients with stage II CRC, which can facilitate individualised management of patients.
引用
收藏
页码:410 / 417
页数:8
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